PHARMACEUTICAL COMPOSITION OF SELECTIVE HCV NS3/4A INHIBITORS
The present invention is directed to compositions comprising the HCV NS3/4A inhibitor, (1aR,5S,8S,10R,22aR)-5-tert-butyl-N-{(1R,2S)-1-[(cyclopropylsulfonyl)carbamoyl]-2-ethenylcyclopro-pyl}-14-methoxy-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocyclopropa[18,19][1,10,3,6]dioxa-diazacyclononadecino[11,12-b]quinoxaline-8-carboxamide, or a pharmaceutically acceptable salt thererof, an oral absorption enhancing polymer, and, optionally, a surfactant. The present invention is also directed to solid dispersions and pharmaceutical compositions containing or made from these compositions, and the methods for making these solid dispersions and pharmaceutical compositions.
1 . A composition comprising:
a) 1aR,5S,8S,10R,22aR)-5-tert-butyl-N-{(1R,2S)-1-[(cyclopropylsulfonyl)carbamoyl]-2-ethenylcyclopropyl}-14-methoxy-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocyclopropa[18,19][1,10,3,6]dioxadiazacyclononadecino[11,12-b]quinoxaline-8-carboxamide (Compound 1), or a pharmaceutically acceptable salt thereof, in a concentration from 0.1% to 40% w/w; and
b) an absorption enhancing polymer in a concentration between 60% and 99.9% w/w.
2 . The composition of claim 1 , wherein Compound 1, or a pharmaceutically acceptable salt thereof, is present at a concentration from 5% to 35%.
3 - 5 . (canceled)
6 . The composition of any of claims 1 - 2 , further comprising a surfactant in a concentration from 2% to 15%.
7 . The composition of claim 6 , wherein the absorption enhancing polymer is a cellulosic polymer or a copolymer of vinyl pyrrolidone and vinyl acetate.
8 . The composition of claim 7 , wherein the absorption enhancing polymer is a cellulosic polymer selected from HPMC or HPMCAS.
9 . The composition of claim 7 , wherein the copolymer of vinyl pyrrolidone and vinyl acetate is copovidone.
10 . (canceled)
11 . The composition of claim 6 , wherein the surfactant is present at a concentration from 5% to 10% w/w and is selected from sodium lauryl sulfate (SLS) and D-α-tocopheryl polyethylene glycol 1000 succinate (vitamin E TPGS).
12 . The composition of claim 1 , wherein the composition is in the form of a particle.
13 . A solid dispersion comprising particles of claim 12 .
14 . The solid dispersion of claim 13 , wherein said dispersion is formed by spray drying or extruding the composition of claim 1 .
15 . The solid dispersion of claim 13 , wherein said dispersion comprises particles wherein the particle further comprises SLS and is formed by spray drying in a mixed solvent system comprising a volatile solvent and a non-volatile solvent.
16 . The solid dispersion of claim 15 , wherein the volatile solvent is ethanol, methanol or acetone and the non-volatile solvent is water.
17 - 18 . (canceled)
19 . A blended material comprising the solid dispersion of claim 15 , a salt, and a disintegrant present at a concentration of 5-20% w/w.
20 . A pharmaceutical formulation comprising the solid dispersion of claim 15 , a salt, and a disintegrant present at a concentration of 5-20% w/w.
21 . The pharmaceutical formulation of claim 20 wherein the salt is selected from NaCl, KCl, CaCl 2 or a combination thereof.
22 . (canceled)
23 . The the pharmaceutical formulation of claim 20 wherein the disintegrant is croscarmellose sodium.
24 - 26 . (canceled)
27 . A process for preparing a solid pharmaceutical composition comprising the steps of:
a) dissolving the composition of a solvent system comprising a volatile solvent;
b) spray-drying the dissolved composition to form particles; and
c) compressing the particles into a tablet or filling into a capsule.
28 . The process of claim 27 comprising the steps of:
a) dissolving the composition of claim 1 in a solvent system comprising a volatile solvent;
b) spray-drying the dissolved composition to form particles;
c) blending the particles with one or more of a diluent, disintegrant, salt, lubricant, and glidant;
d) subjecting the blended particles to roller compaction;
e) adding a lubricant; and
f) compressing the particles into a tablet or capsule.
29 . (canceled)
30 . The process of wherein the solvent system further comprises a non-volatile solvent.
31 . (canceled)
32 . The process of claim 27 , wherein the solvent system is acetone:water (90:10).